CN103311540A - Lithium ion battery anode material and preparation method thereof - Google Patents
Lithium ion battery anode material and preparation method thereof Download PDFInfo
- Publication number
- CN103311540A CN103311540A CN2013102012174A CN201310201217A CN103311540A CN 103311540 A CN103311540 A CN 103311540A CN 2013102012174 A CN2013102012174 A CN 2013102012174A CN 201310201217 A CN201310201217 A CN 201310201217A CN 103311540 A CN103311540 A CN 103311540A
- Authority
- CN
- China
- Prior art keywords
- lithium
- anode material
- preparation
- ion batteries
- salt
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
Images
Classifications
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
- Y02E60/00—Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
- Y02E60/10—Energy storage using batteries
Landscapes
- Battery Electrode And Active Subsutance (AREA)
Abstract
The invention discloses a lithium ion battery anode material and a preparation method thereof. The anode material comprises lithium nickel manganese oxide, and is doped with one or more metal Xs, wherein the metal Xs are one or more of lutetium Lu, ytterbium Yb, gallium Ga and zirconium Zr; the chemical general formula of the anode material is LiNi0.5Mn1.5-aXaO4, wherein a is larger than 0 and smaller than or equal to 0.03. The lithium ion battery anode material prepared through the preparation method is uniform in element mixing, regular in structure and good in cycle performance, so that the performance of a lithium ion battery is improved.
Description
Technical field
The present invention relates to technical field of lithium ion, relate in particular to a kind of anode material for lithium-ion batteries and preparation method thereof.
Background technology
At present, chemical power source more and more is subject to people's attention, and especially lithium ion battery because of its height ratio capacity, high-specific-power, long-life, environment amenable characteristics, becomes the focus that people pay close attention to.In lithium ion battery, positive electrode is its core, is absolute lithium ion battery chemical property, security performance and the principal element that further develops thereof.
The development of anode material for lithium-ion batteries is the principal element that the restriction lithium ion battery further enlarges application, and the coml anode material for lithium-ion batteries mainly contains cobalt acid lithium, LiMn2O4, ternary material etc., but all can not satisfy the demand of current development fully.Cobalt acid lithium specific capacity height, cycle performance is better, but manufacturing cost is expensive and have a potential safety hazard; The LiFePO4 security performance is good, but specific capacity is lower, and high rate performance is poor; The LiMn2O4 cost is low, and cryogenic property is good, but energy density is low, and high temperature cyclic performance is poor; Ternary material energy density height, good cycle, but exist potential safety hazard and current potential platform lower.
Summary of the invention
The purpose of this invention is to provide a kind of anode material for lithium-ion batteries and preparation method thereof, the anode material for lithium-ion batteries element that makes by this preparation method mixes more even, structure is more regular, and cycle performance is good, and then has improved the performance of lithium ion battery.
The objective of the invention is to be achieved through the following technical solutions, a kind of anode material for lithium-ion batteries, described positive electrode comprises the nickel LiMn2O4, and is doped with the material of one or more metal X, and wherein said metal X is one or more among lutetium Lu, ytterbium Yb, gallium Ga, the zirconium Zr;
The chemical general formula of described positive electrode is LiNi
0.5Mn
1.5-aX
aO
4,, 0＜a≤0.03.
A kind of preparation method of anode material for lithium-ion batteries, described preparation method comprises:
(1) with the compound of solubility lithium salts, soluble nickel salt, soluble manganese salt and metal X source element and the acid solution of ammonium, be 1:0.5:(1.5-a in molar ratio): the consumption mixed dissolution of a:3 is in deionized water, be made into mixed solution, 0＜a≤0.03 wherein, described metal X is one or more among lutetium Lu, ytterbium Yb, gallium Ga, the zirconium Zr;
(2) the mixed solution continuous evaporate to dryness that stirs under 60-80 ℃ with step (1) preparation obtains gel;
(3) it is very fast dry under 110 ℃ that the gel that step (2) is produced is transferred to vacuum drying chamber fast;
(4) desiccant gel of step (3) gained is transferred in the Muffle furnace at 300-400 ℃ of presintering 3-5h, heating rate is 2-10 ℃/s during pre-burning;
(5) subsequently at 800-900 ℃ of following double sintering 10-15h, oxygenating gas and heating rate in good time in the double sintering process are 1-10 ℃/s, and naturally cool to room temperature;
(6) product with step (5) gained grinds, sieves, and obtains described anode material for lithium-ion batteries.
Described solubility lithium salts is one or more of lithium sulfate, lithium nitrate, lithium acetate, lithium chloride.
Described soluble nickel salt is one or more of nickelous sulfate, nickel nitrate, nickel acetate, nickel chloride.
Described soluble manganese salt is one or more of manganese sulfate, manganese nitrate, manganese acetate, manganese chloride.
The compound of described metal X source element is the soluble-salt of described metal X, wherein:
Solubility lutetium salt is one or both of lutecium chloride, sulfuric acid lutetium; Solubility ytterbium salt is one or more of ytterbium nitrate, ytterbium sulfate, ytterbium chloride; Solubility gallium salt is one or both of gallium nitrate, gallium chloride; The solubility zirconates is one or more of zirconium nitrate, zirconium chloride, zirconium acetate.
The acid solution of ammonium described in the step (1) comprises one or more of ammonium oxalate, ammonium citrate, malic acid ammonium.
As seen from the above technical solution provided by the invention, described positive electrode comprises the nickel LiMn2O4, and is doped with the material of one or more metal X, and wherein said metal X is one or more among lutetium Lu, ytterbium Yb, gallium Ga, the zirconium Zr; The chemical general formula of this positive electrode is LiNi
0.5Mn
1.5-aX
aO
4,, 0＜a≤0.03.More even by the anode material for lithium-ion batteries element mixing that this preparation method makes, structure is more regular, and cycle performance is good, and then has improved the performance of lithium ion battery.
Description of drawings
In order to be illustrated more clearly in the technical scheme of the embodiment of the invention, the accompanying drawing of required use is done to introduce simply in will describing embodiment below, apparently, accompanying drawing in describing below only is some embodiments of the present invention, for those of ordinary skill in the art, under the prerequisite of not paying creative work, can also obtain other accompanying drawings according to these accompanying drawings.
Fig. 1 provides preparation method's schematic flow sheet of anode material for lithium-ion batteries for the embodiment of the invention;
The cycle performance schematic diagram of button cell is provided for the positive electrode that utilizes the embodiment of the invention to provide Fig. 2.
Embodiment
Below in conjunction with the accompanying drawing in the embodiment of the invention, the technical scheme in the embodiment of the invention is clearly and completely described, obviously, described embodiment only is the present invention's part embodiment, rather than whole embodiment.Based on embodiments of the invention, those of ordinary skills belong to protection scope of the present invention not making the every other embodiment that obtains under the creative work prerequisite.
The embodiment of the invention provides a kind of anode material for lithium-ion batteries, and described positive electrode comprises the nickel LiMn2O4, and is doped with the material of one or more metal X, and wherein said metal X is one or more among lutetium Lu, ytterbium Yb, gallium Ga, the zirconium Zr;
The chemical general formula of described positive electrode is LiNi
0.5Mn
1.5-aX
aO
4,, 0＜a≤0.03.
Below in conjunction with accompanying drawing the embodiment of the invention is described in further detail, is illustrated in figure 1 as preparation method's schematic flow sheet that the embodiment of the invention provides anode material for lithium-ion batteries, described preparation method comprises:
(1) with the compound of solubility lithium salts, soluble nickel salt, soluble manganese salt and metal X source element and the acid solution of ammonium, be 1:0.5:(1.5-a in molar ratio): the consumption mixed dissolution of a:3 is in deionized water, be made into mixed solution, 0＜a≤0.03 wherein, described metal X is one or more among lutetium Lu, ytterbium Yb, gallium Ga, the zirconium Zr;
In this step (1), described solubility lithium salts can be one or more of lithium sulfate, lithium nitrate, lithium acetate, lithium chloride; Described soluble nickel salt is one or more of nickelous sulfate, nickel nitrate, nickel acetate, nickel chloride; Described soluble manganese salt is one or more of manganese sulfate, manganese nitrate, manganese acetate, manganese chloride.
And the compound of described metal X source element is the soluble-salt of described metal X, wherein:
Solubility lutetium salt is one or both of lutecium chloride, sulfuric acid lutetium; Solubility ytterbium salt is one or more of ytterbium nitrate, ytterbium sulfate, ytterbium chloride; Solubility gallium salt is one or both of gallium nitrate, gallium chloride; The solubility zirconates is one or more of zirconium nitrate, zirconium chloride, zirconium acetate.
In addition, the acid solution of ammonium described in the above-mentioned steps can also comprise one or more of ammonium oxalate, ammonium citrate, malic acid ammonium.
The acid solution of described ammonium comprises one or more of ammonium oxalate, ammonium citrate, malic acid ammonium.
(2) the mixed solution continuous evaporate to dryness that stirs under 60-80 ℃ with step (1) preparation obtains gel;
(3) it is very fast dry under 110 ℃ that the gel that step (2) is produced is transferred to vacuum drying chamber fast;
(4) desiccant gel of step (3) gained is transferred in the Muffle furnace at 300-400 ℃ of presintering 3-5h, heating rate is 2-10 ℃/s during pre-burning;
(5) subsequently at 800-900 ℃ of following double sintering 10-15h, oxygenating gas and heating rate in good time in the double sintering process are 1-10 ℃/s, and naturally cool to room temperature;
(6) product with step (5) gained grinds, sieves, and obtains described anode material for lithium-ion batteries.
Further, can also utilize above-mentioned resulting anode material for lithium-ion batteries to make lithium ion cell positive, and be assembled into corresponding lithium ion battery, specifically be with cell positive material LiNi
0.5Mn
1.5-aX
aO
4, acetylene black, PVDF is according to mass ratio 8:1:1 weighing, with the N-methyl pyrrolidone as solvent, mix to stir and size mixing, apply with the collector of aluminium foil as positive electrode, being cut into disk after super-dry, is that negative pole, polypropylene microporous film are barrier film, 1.0mol/L LiPF then with the lithium metal
6EC+DMC (v:v=1:1) is electrolyte, is being full of assembled battery in the glove box of argon gas, carries out the electrochemical property test of battery then.
For instance, the cycle performance schematic diagram that the positive electrode that utilizes the embodiment of the invention to provide is assembled into button cell is provided, by the cycle performance of battery among Fig. 2 as can be known: owing to adopted the doping of at least a other metal ions, strengthened the charge-discharge performance of nickel manganate cathode material for lithium, suppress the John-Teller effect, thereby obtained the high performance lithium ion battery anode material nickel LiMn2O4 that cycle performance is good, structure is more stable.
Come the preparation process of above-mentioned positive electrode is described with concrete example more below:
Embodiment 1:
The preparation chemical formula is LiNi
0.5Mn
1.47Lu
0.03O
4The nickel manganate cathode material for lithium.At first the ammonium oxalate that takes by weighing 1mol lithium nitrate, 0.5mol nickel nitrate, 1.47mol manganese nitrate, 0.03mol sulfuric acid lutetium and 3mol by stoichiometric proportion adds in the deionized water of 500ml, stirs until obtaining wet gel down in 60 ℃;
Wet gel is put in the vacuum drying chamber, obtains xerogel in 110 ℃ of following dryings, then xerogel is transferred in the Muffle furnace, in 400 ℃ of following presintering 4h, the heating rate of presintering is 2 ℃/s, is warming up to 800 ℃ of calcining 15h in the speed with 1 ℃/s, and in good time supplemental oxygen.
Naturally cool to room temperature, grinding sieves obtains high performance lithium ion battery anode material.
Again the gained material is assembled into as stated above button cell and under the 1C multiplying power, carries out the constant current charge-discharge performance test.
Embodiment 2:
The preparation chemical formula is LiNi
0.5Mn
1.48Lu
0.01Zr
0.01O
4The nickel manganate cathode material for lithium.At first the malic acid ammonium that takes by weighing 1mol lithium sulfate, 0.5mol nickel acetate, 1.48mol manganese nitrate, 0.01mol lutecium chloride, 0.01mol zirconium nitrate and 3mol by stoichiometric proportion adds in the deionized water of 500ml, stirs until obtaining wet gel down in 80 ℃;
Wet gel is put in the vacuum drying chamber, obtains xerogel in 110 ℃ of following dryings, then xerogel is transferred in the Muffle furnace, in 400 ℃ of following presintering 4h, the heating rate of presintering is 10 ℃/s, is warming up to 900 ℃ of calcining 15h in the speed with 10 ℃/s, and in good time supplemental oxygen.
Naturally cool to room temperature, grinding sieves obtains high performance lithium ion battery anode material.
Again the gained material is assembled into as stated above button cell and under the 1C multiplying power, carries out the constant current charge-discharge performance test.
Embodiment 3:
The preparation chemical formula is LiNi
0.5Mn
1.47Lu
0.01Zr
0.01Yb
0.01O
4The nickel manganate cathode material for lithium.At first the ammonium citrate that takes by weighing 1mol lithium sulfate, 0.5mol nickel nitrate, 1.47mol manganese acetate, 0.01mol sulfuric acid lutetium, 0.01mol zirconium nitrate, 0.01mol ytterbium chloride and 3mol by stoichiometric proportion adds in the deionized water of 500ml, stirs until obtaining wet gel down in 70 ℃;
Wet gel is put in the vacuum drying chamber, obtains xerogel in 110 ℃ of following dryings, then xerogel is transferred in the Muffle furnace, in 300 ℃ of following presintering 5h, the heating rate of presintering is 5 ℃/s, is warming up to 900 ℃ of calcining 15h in the speed with 6 ℃/s, and in good time supplemental oxygen.
Naturally cool to room temperature, grinding sieves obtains high performance lithium ion battery anode material.
Again the gained material is assembled into as stated above button cell and under the 1C multiplying power, carries out the constant current charge-discharge performance test.
Embodiment 4:
The preparation chemical formula is LiNi
0.5Mn
1.48Lu
0.005Zr
0.005Yb
0.005Ga
0.005O
4The nickel manganate cathode material for lithium.At first the ammonium oxalate that takes by weighing 1mol lithium acetate, 0.5mol nickelous sulfate, 1.48mol manganese nitrate, 0.005mol lutecium chloride, 0.005mol zirconium chloride, 0.005mol ytterbium sulfate, 0.005mol gallium nitrate and 3mol by stoichiometric proportion adds in the deionized water of 500ml, stirs until obtaining wet gel down in 70 ℃;
Wet gel is put in the vacuum drying chamber, obtains xerogel in 110 ℃ of following dryings, then xerogel is transferred in the Muffle furnace, in 300 ℃ of following presintering 5h, the heating rate of presintering is 3 ℃/s, is warming up to 900 ℃ of calcining 15h in the speed with 5 ℃/s, and in good time supplemental oxygen.
Naturally cool to room temperature, grinding sieves obtains high performance lithium ion battery anode material.
Again the gained material is assembled into as stated above button cell and under the 1C multiplying power, carries out the constant current charge-discharge performance test.
In sum, more even by the anode material for lithium-ion batteries element mixing that the invention described above embodiment preparation method makes, structure is more regular, and cycle performance is good, and then has improved the performance of lithium ion battery.
The above; only for the preferable embodiment of the present invention, but protection scope of the present invention is not limited thereto, and anyly is familiar with those skilled in the art in the technical scope that the present invention discloses; the variation that can expect easily or replacement all should be encompassed within protection scope of the present invention.Therefore, protection scope of the present invention should be as the criterion with the protection range of claims.
Claims (7)
1. an anode material for lithium-ion batteries is characterized in that, described positive electrode comprises the nickel LiMn2O4, and is doped with the material of one or more metal X, and wherein said metal X is one or more among lutetium Lu, ytterbium Yb, gallium Ga, the zirconium Zr;
The chemical general formula of described positive electrode is LiNi
0.5Mn
1.5-aX
aO
4,, 0＜a≤0.03.
2. the preparation method of an anode material for lithium-ion batteries is characterized in that, described preparation method comprises:
(1) with the compound of solubility lithium salts, soluble nickel salt, soluble manganese salt and metal X source element and the acid solution of ammonium, be 1:0.5:(1.5-a in molar ratio): the consumption mixed dissolution of a:3 is in deionized water, be made into mixed solution, 0＜a≤0.03 wherein, described metal X is one or more among lutetium Lu, ytterbium Yb, gallium Ga, the zirconium Zr;
(2) the mixed solution continuous evaporate to dryness that stirs under 60-80 ℃ with step (1) preparation obtains gel;
(3) it is very fast dry under 110 ℃ that the gel that step (2) is produced is transferred to vacuum drying chamber fast;
(4) desiccant gel of step (3) gained is transferred in the Muffle furnace at 300-400 ℃ of presintering 3-5h, heating rate is 2-10 ℃/s during pre-burning;
(5) subsequently at 800-900 ℃ of following double sintering 10-15h, oxygenating gas and heating rate in good time in the double sintering process are 1-10 ℃/s, and naturally cool to room temperature;
(6) product with step (5) gained grinds, sieves, and obtains described anode material for lithium-ion batteries.
3. as the preparation method of anode material for lithium-ion batteries as described in the claim 2, it is characterized in that,
Described solubility lithium salts is one or more of lithium sulfate, lithium nitrate, lithium acetate, lithium chloride.
4. as the preparation method of anode material for lithium-ion batteries as described in the claim 2, it is characterized in that,
Described soluble nickel salt is one or more of nickelous sulfate, nickel nitrate, nickel acetate, nickel chloride.
5. as the preparation method of anode material for lithium-ion batteries as described in the claim 2, it is characterized in that,
Described soluble manganese salt is one or more of manganese sulfate, manganese nitrate, manganese acetate, manganese chloride.
6. as the preparation method of anode material for lithium-ion batteries as described in the claim 2, it is characterized in that the compound of described metal X source element is the soluble-salt of described metal X, wherein:
Solubility lutetium salt is one or both of lutecium chloride, sulfuric acid lutetium; Solubility ytterbium salt is one or more of ytterbium nitrate, ytterbium sulfate, ytterbium chloride; Solubility gallium salt is one or both of gallium nitrate, gallium chloride; The solubility zirconates is one or more of zirconium nitrate, zirconium chloride, zirconium acetate.
7. as the preparation method of anode material for lithium-ion batteries as described in the claim 2, it is characterized in that,
The acid solution of ammonium described in the step (1) comprises one or more of ammonium oxalate, ammonium citrate, malic acid ammonium.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN201310201217.4A CN103311540B (en) | 2013-05-27 | 2013-05-27 | A kind of anode material for lithium-ion batteries and preparation method thereof |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN201310201217.4A CN103311540B (en) | 2013-05-27 | 2013-05-27 | A kind of anode material for lithium-ion batteries and preparation method thereof |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN103311540A true CN103311540A (en) | 2013-09-18 |
| CN103311540B CN103311540B (en) | 2016-01-20 |
Family
ID=49136518
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN201310201217.4A Expired - Fee Related CN103311540B (en) | 2013-05-27 | 2013-05-27 | A kind of anode material for lithium-ion batteries and preparation method thereof |
Country Status (1)
| Country | Link |
|---|---|
| CN (1) | CN103311540B (en) |
Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN104201370A (en) * | 2014-07-16 | 2014-12-10 | 北京好风光储能技术有限公司 | Positive electrode material of lithium ion battery, and preparation method thereof |
| CN106784720A (en) * | 2017-01-08 | 2017-05-31 | 合肥国轩高科动力能源有限公司 | High-performance manganese-based lithium ion battery positive electrode material and preparation method thereof |
| CN107834054A (en) * | 2017-12-19 | 2018-03-23 | 宁波高新区锦众信息科技有限公司 | A kind of preparation method of lithium ion battery nickel manganese lithium graphene composite material |
| CN107946551A (en) * | 2017-10-20 | 2018-04-20 | 合肥国轩高科动力能源有限公司 | Doped lithium nickel manganese oxide material, modified lithium nickel manganese oxide positive electrode material and preparation method thereof |
| CN109037612A (en) * | 2018-07-04 | 2018-12-18 | 合肥国轩高科动力能源有限公司 | Scandium-doped lithium nickel manganese oxide lithium ion battery positive electrode material and preparation method thereof |
| CN109935798A (en) * | 2017-12-19 | 2019-06-25 | 宁波高新区锦众信息科技有限公司 | A kind of preparation method of lithium ion battery nickel manganese lithium composite material |
| CN113955805A (en) * | 2021-09-03 | 2022-01-21 | 西安电子科技大学 | Lithium-rich cathode material of lithium ion battery and preparation method thereof |
Citations (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN1667865A (en) * | 2004-03-12 | 2005-09-14 | 三星Sdi株式会社 | Lithium secondary battery |
| CN101133513A (en) * | 2005-06-14 | 2008-02-27 | 松下电器产业株式会社 | Nonaqueous electrolyte secondary battery |
| CN101320807A (en) * | 2008-07-04 | 2008-12-10 | 深圳市贝特瑞新能源材料股份有限公司 | Positive electrode material of multi-component composite lithium ion cell and its preparation method |
| CN101388448A (en) * | 2006-09-14 | 2009-03-18 | 日产自动车株式会社 | Positive electrode for non-aqueous electrolyte secondary battery and non-aqueous electrolyte secondary battery using the same |
| CN102088087A (en) * | 2010-12-31 | 2011-06-08 | 华南师范大学 | Lithium ion battery anode material doped with rare earth elements and preparation method thereof |
| US20120028128A1 (en) * | 2009-03-18 | 2012-02-02 | Santoku Corporation | All-solid-state lithium battery |
| CN102723481A (en) * | 2012-07-09 | 2012-10-10 | 华南师范大学 | High-voltage lithium battery cathode material doped with trace amount of tungsten and preparation method thereof |
-
2013
- 2013-05-27 CN CN201310201217.4A patent/CN103311540B/en not_active Expired - Fee Related
Patent Citations (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN1667865A (en) * | 2004-03-12 | 2005-09-14 | 三星Sdi株式会社 | Lithium secondary battery |
| CN101133513A (en) * | 2005-06-14 | 2008-02-27 | 松下电器产业株式会社 | Nonaqueous electrolyte secondary battery |
| CN101388448A (en) * | 2006-09-14 | 2009-03-18 | 日产自动车株式会社 | Positive electrode for non-aqueous electrolyte secondary battery and non-aqueous electrolyte secondary battery using the same |
| CN101320807A (en) * | 2008-07-04 | 2008-12-10 | 深圳市贝特瑞新能源材料股份有限公司 | Positive electrode material of multi-component composite lithium ion cell and its preparation method |
| US20120028128A1 (en) * | 2009-03-18 | 2012-02-02 | Santoku Corporation | All-solid-state lithium battery |
| CN102088087A (en) * | 2010-12-31 | 2011-06-08 | 华南师范大学 | Lithium ion battery anode material doped with rare earth elements and preparation method thereof |
| CN102723481A (en) * | 2012-07-09 | 2012-10-10 | 华南师范大学 | High-voltage lithium battery cathode material doped with trace amount of tungsten and preparation method thereof |
Cited By (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN104201370A (en) * | 2014-07-16 | 2014-12-10 | 北京好风光储能技术有限公司 | Positive electrode material of lithium ion battery, and preparation method thereof |
| CN104201370B (en) * | 2014-07-16 | 2016-10-05 | 北京好风光储能技术有限公司 | A kind of anode material for lithium-ion batteries and preparation method thereof |
| CN106784720A (en) * | 2017-01-08 | 2017-05-31 | 合肥国轩高科动力能源有限公司 | High-performance manganese-based lithium ion battery positive electrode material and preparation method thereof |
| CN107946551A (en) * | 2017-10-20 | 2018-04-20 | 合肥国轩高科动力能源有限公司 | Doped lithium nickel manganese oxide material, modified lithium nickel manganese oxide positive electrode material and preparation method thereof |
| CN107946551B (en) * | 2017-10-20 | 2020-07-17 | 合肥国轩高科动力能源有限公司 | Doped lithium nickel manganese oxide material, modified lithium nickel manganese oxide positive electrode material and preparation method thereof |
| CN107834054A (en) * | 2017-12-19 | 2018-03-23 | 宁波高新区锦众信息科技有限公司 | A kind of preparation method of lithium ion battery nickel manganese lithium graphene composite material |
| CN109935798A (en) * | 2017-12-19 | 2019-06-25 | 宁波高新区锦众信息科技有限公司 | A kind of preparation method of lithium ion battery nickel manganese lithium composite material |
| CN109037612A (en) * | 2018-07-04 | 2018-12-18 | 合肥国轩高科动力能源有限公司 | Scandium-doped lithium nickel manganese oxide lithium ion battery positive electrode material and preparation method thereof |
| CN113955805A (en) * | 2021-09-03 | 2022-01-21 | 西安电子科技大学 | Lithium-rich cathode material of lithium ion battery and preparation method thereof |
Also Published As
| Publication number | Publication date |
|---|---|
| CN103311540B (en) | 2016-01-20 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CN104157831B (en) | Lithium-rich manganese-based composite positive pole of the spinel nickel LiMn2O4 of a kind of core shell structure, stratiform and preparation method thereof | |
| CN106340638B (en) | A kind of high-rate lithium-rich manganese-based anode material of double layer hollow structure and preparation method thereof | |
| CN109980219A (en) | Full gradient nickel cobalt manganese anode material, ruthenium-oxide covering material and preparation method thereof | |
| CN103441265B (en) | Rich lithium composite positive pole of a kind of codope and preparation method thereof | |
| CN103474625B (en) | Novel lithium ion battery anode material coating method with core-shell structure | |
| CN103474650B (en) | Method for preparing hollow high voltage nickel manganese acid lithium anode material | |
| CN103311540B (en) | A kind of anode material for lithium-ion batteries and preparation method thereof | |
| US11198621B2 (en) | Lithium-rich layered oxide material with phase structure gradient and its preparation method | |
| CN104134790B (en) | A kind of nickle cobalt lithium manganate is material modified and preparation method thereof and application | |
| CN104835955B (en) | A kind of lithium ion battery nickle cobalt lithium manganate composite positive pole and preparation method thereof | |
| CN107910529A (en) | A kind of ternary cathode material of lithium ion battery of manganese Base Metal organic frame compound cladding and preparation method thereof | |
| CN103094554B (en) | Modified lithium manganate anode material and preparation method thereof | |
| CN104638227A (en) | Method for modifying positive electrode material of lithium ion battery | |
| CN102437323A (en) | Anode material of lithium ion battery and preparation method thereof | |
| CN105098158B (en) | A kind of lithium-enriched cathodic material of lithium ion battery of zirconium doping and preparation method thereof | |
| CN103151528A (en) | Method for preparing aluminum-doped zinc oxide coated lithium-ion battery positive-pole material | |
| CN107302083A (en) | A kind of solid reaction process preparation method of nickel lithium manganate cathode material | |
| CN104332619A (en) | Polypyrrole- coated full-gradient cathode material and preparation method thereof | |
| CN108091854A (en) | A kind of high-voltage spinel type anode material for lithium-ion batteries of Anion-cation multiple dope and preparation method thereof | |
| CN104852040B (en) | A kind of preparation method of the nickel lithium manganate cathode material of high multiplying power lithium ion battery | |
| CN106450285A (en) | Preparation method capable of increasing electrochemical performance of magnesium-sodium-doped lithium permanganate anode material | |
| CN105304894A (en) | Method for preparing high-performance lithium manganite positive electrode material by compound doping | |
| CN106654255A (en) | Aluminum-doped and modified cathode material for high-capacity lithium ion batteries | |
| CN103872313B (en) | Anode material for lithium-ion batteries LiMn2‑2xM(II)xSixO4And preparation method thereof | |
| CN106784657A (en) | A kind of method that sodium and iron codope prepare High-performance lithium manganate anode material |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| C06 | Publication | ||
| PB01 | Publication | ||
| C10 | Entry into substantive examination | ||
| SE01 | Entry into force of request for substantive examination | ||
| C14 | Grant of patent or utility model | ||
| GR01 | Patent grant | ||
| CF01 | Termination of patent right due to non-payment of annual fee | ||
| CF01 | Termination of patent right due to non-payment of annual fee |
Granted publication date: 20160120 Termination date: 20200527 |